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2pgg

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==Overview==
==Overview==
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Single-subunit polymerases are universally encoded in both cellular, organisms and viruses. Their three-dimensional structures have the shape, of a right-hand with the active site located in the palm region, which has, a topology similar to that of the RNA recognition motif (RRM) found in, many RNA-binding proteins. Considering that polymerases have well, conserved structures, it was surprising that the RNA-dependent RNA, polymerases from birnaviruses, a group of dsRNA viruses, have their, catalytic motifs arranged in a permuted order in sequence. Here we report, the 2.5 A structure of a birnavirus VP1 in which the polymerase palm, subdomain adopts a new active site topology that has not been previously, observed in other polymerases. In addition, the polymerase motif C of VP1, has the sequence of -ADN-, a highly unusual feature for RNA-dependent, polymerases. Through site-directed mutagenesis, we have shown that, changing the VP1 motif C from -ADN- to -GDD- results in a mutant with an, increased RNA synthesis activity. Our results indicate that the active, site topology of VP1 may represent a newly developed branch in polymerase, evolution, and that birnaviruses may have acquired the -ADN- mutation to, control their growth rate.
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Single-subunit polymerases are universally encoded in both cellular organisms and viruses. Their three-dimensional structures have the shape of a right-hand with the active site located in the palm region, which has a topology similar to that of the RNA recognition motif (RRM) found in many RNA-binding proteins. Considering that polymerases have well conserved structures, it was surprising that the RNA-dependent RNA polymerases from birnaviruses, a group of dsRNA viruses, have their catalytic motifs arranged in a permuted order in sequence. Here we report the 2.5 A structure of a birnavirus VP1 in which the polymerase palm subdomain adopts a new active site topology that has not been previously observed in other polymerases. In addition, the polymerase motif C of VP1 has the sequence of -ADN-, a highly unusual feature for RNA-dependent polymerases. Through site-directed mutagenesis, we have shown that changing the VP1 motif C from -ADN- to -GDD- results in a mutant with an increased RNA synthesis activity. Our results indicate that the active site topology of VP1 may represent a newly developed branch in polymerase evolution, and that birnaviruses may have acquired the -ADN- mutation to control their growth rate.
==About this Structure==
==About this Structure==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Pan, J.]]
[[Category: Pan, J.]]
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[[Category: Tao, Y.J.]]
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[[Category: Tao, Y J.]]
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[[Category: Vakharia, V.N.]]
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[[Category: Vakharia, V N.]]
[[Category: birnavirus]]
[[Category: birnavirus]]
[[Category: dsrna virus]]
[[Category: dsrna virus]]
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[[Category: rdrp]]
[[Category: rdrp]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 14:53:39 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 18:29:15 2008''

Revision as of 16:29, 21 February 2008


2pgg, resolution 2.50Å

Drag the structure with the mouse to rotate

Crystal Structure of a Birnavirus (IBDV) RNA-dependent RNA Polymerase VP1

Overview

Single-subunit polymerases are universally encoded in both cellular organisms and viruses. Their three-dimensional structures have the shape of a right-hand with the active site located in the palm region, which has a topology similar to that of the RNA recognition motif (RRM) found in many RNA-binding proteins. Considering that polymerases have well conserved structures, it was surprising that the RNA-dependent RNA polymerases from birnaviruses, a group of dsRNA viruses, have their catalytic motifs arranged in a permuted order in sequence. Here we report the 2.5 A structure of a birnavirus VP1 in which the polymerase palm subdomain adopts a new active site topology that has not been previously observed in other polymerases. In addition, the polymerase motif C of VP1 has the sequence of -ADN-, a highly unusual feature for RNA-dependent polymerases. Through site-directed mutagenesis, we have shown that changing the VP1 motif C from -ADN- to -GDD- results in a mutant with an increased RNA synthesis activity. Our results indicate that the active site topology of VP1 may represent a newly developed branch in polymerase evolution, and that birnaviruses may have acquired the -ADN- mutation to control their growth rate.

About this Structure

2PGG is a Single protein structure of sequence from Infectious bursal disease virus. Active as RNA-directed RNA polymerase, with EC number 2.7.7.48 Full crystallographic information is available from OCA.

Reference

The structure of a birnavirus polymerase reveals a distinct active site topology., Pan J, Vakharia VN, Tao YJ, Proc Natl Acad Sci U S A. 2007 May 1;104(18):7385-90. Epub 2007 Apr 24. PMID:17456597

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